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Efficacy and Safety of Mucopolysaccharide Polysulfate in Treating Moderate to Severe Post-inflammatory Hyperpigmentation from Acne Vulgaris

Efficacy and Safety of Mucopolysaccharide Polysulfate in Treating Moderate to Severe Post-inflammatory Hyperpigmentation from Acne Vulgaris

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124476
Enrollment
Unknown
Registered
2026-05-13
Start date
2026-05-18
Completion date
Unknown
Last updated
2026-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-inflammatory Hyperpigmentation (PIH) from Acne Vulgaris

Interventions

Control Group:Patients with moderate (Grade III) or severe (Grade IV) acne, receiving oral doxycycline tablets and topical clindamycin phosphate gel, twice daily for 12 weeks.
Experimental Group:Patients with moderate (Grade III) or severe (Grade IV) acne, receiving oral doxycycline tablets, topical clindamycin phosphate gel, and topical mucopolysaccharide polysulfate cream
PIH Treatment Group:Patients who developed PIH after treatment with oral doxycycline tablets and topical clindamycin phosphate gel, receiving topical mucopolysaccharide polysulfate cream, twice daily

Sponsors

The First Affiliated Hospital of Guilin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.Age 14-35 years, male or female. 2.Clinically diagnosed with acne vulgaris according to the "Chinese Guidelines for the Treatment of Acne (2024 Revision)", with facial characteristics meeting the following criteria: 30-75 inflammatory lesions (papules, pustules); 30-100 non-inflammatory lesions (open and closed comedones); and total nodule count = 2. 3.Patients with moderate (Grade III) or severe (Grade IV) acne vulgaris according to the modified Pillsbury classification. 4.Voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating female patients. 2.Patients with acne conglobata or acne fulminans. 3.Patients who have received treatment with immunosuppressants, antibiotics, or corticosteroids within 1 month prior to the study. 4.Patients with liver, kidney, hematological, or other visceral diseases. 5.Patients with known allergies to any components of the study medication.

Design outcomes

Primary

MeasureTime frame
Change in Melanin Level;Change in Hemoglobin Level;Serious Adverse Events (SAE);

Secondary

MeasureTime frame
Change in Transepidermal Water Loss (TEWL);Change in Stratum Corneum Hydration (SCH);Quality of Life Score;Laboratory Indicators;

Countries

China

Contacts

Public ContactYan Wenjie

The First Affiliated Hospital of Guilin Medical University

ywj716@qq.com+86 139 7831 1264

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026